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Structure of 1956331-04-6
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This hydrochloride salt of 2,3-dihydro-4-methyl-1H-isoindole delivers a stable, moisture-tolerant platform for heterocyclic synthesis. The protonated nitrogen enhances reactivity in electrophilic substitution and facilitates downstream functionalization. Ideal for medicinal chemistry applications requiring a rigid, electron-rich aromatic scaffold with tunable basicity.
1H-Isoindole, 2,3-dihydro-4-methyl-, hydrochloride (1:1) serves as a stable, bench-ready building block for the synthesis of functionalized isoindoline derivatives. The hydrochloride salt enhances solubility and handling while preserving reactivity in standard coupling and electrophilic substitution protocols. Its methyl-substituted core facilitates downstream transformations including palladium-catalyzed cross-couplings and heterocyclization reactions, making it a practical scaffold for medicinal chemistry campaigns requiring nitrogen-containing aromatic systems.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: